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About the Role
Help shape clinical research at ICON plc by becoming a Clinical Transparency Specialist focused on anonymizing trial documents. Your role ensures compliance with transparency regulations.
This position involves managing the anonymization of clinical trial documents, ensuring they comply with regulatory requirements for disclosure. Collaborating with various teams, you will execute plans that minimize re-identification risks and guarantee accurate redaction. Your understanding of clinical transparency will support essential submissions to regulatory authorities in Europe and Canada.
Key Responsibilities:
• Coordinate timely anonymization processes for datasets
• Assess clinical documents against disclosure standards
• Partner with teams to compile necessary datasets
• Craft anonymization strategies according to GDPR
• Conduct quality assurance on anonymized submissions
Requirements:
• Bachelor's in a scientific or technical field
• Minimum 3 years in health...
This position involves managing the anonymization of clinical trial documents, ensuring they comply with regulatory requirements for disclosure. Collaborating with various teams, you will execute plans that minimize re-identification risks and guarantee accurate redaction. Your understanding of clinical transparency will support essential submissions to regulatory authorities in Europe and Canada.
Key Responsibilities:
• Coordinate timely anonymization processes for datasets
• Assess clinical documents against disclosure standards
• Partner with teams to compile necessary datasets
• Craft anonymization strategies according to GDPR
• Conduct quality assurance on anonymized submissions
Requirements:
• Bachelor's in a scientific or technical field
• Minimum 3 years in health...
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